ライフサイエンスコーパス: Lactococcus lactis

1 the pilB gene in the nonpathogenic bacterium Lactococcus lactis.

2 related bacteria, Enterococcus faecalis and Lactococcus lactis.

3 f the otherwise unrelated plasmid pRS01 from Lactococcus lactis.

4 of the regulation of glucose utilization in Lactococcus lactis.

5 for a high-efficiency conjugation process in Lactococcus lactis.

6 es to cellular poles in Escherichia coli and Lactococcus lactis.

7 pressed on the surface of the surrogate host Lactococcus lactis.

8 peptidases from Lactobacillus helveticus and Lactococcus lactis.

9 te with the prototypical family 1A DHOD from Lactococcus lactis.

10 ve studied the bacterial L1.LtrB intron from Lactococcus lactis.

11 beta-hemolytic phenotype to the nonhemolytic Lactococcus lactis.

12 acillus subtilis, Listeria monocytogenes and Lactococcus lactis.

13 isin is an antimicrobial peptide produced by Lactococcus lactis.

14 c that is similar to the nisin-A produced by Lactococcus lactis.

15 showed sequence similarities to LCNDR2 from Lactococcus lactis.

16 of CdnG and Cap5, from Asticcacaulis sp. and Lactococcus lactis.

17 ge and coexist in a culture of the bacterium Lactococcus lactis.

18 of the biotin-specific S component BioY from Lactococcus lactis.

19 fied Shr or intranasally with Shr-expressing Lactococcus lactis.

20 bind specifically to the Class 1A DHOD from Lactococcus lactis, 3,4-dihydroxybenzoate (3,4-diOHB) an

21 ated sex factor that controls conjugation in Lactococcus lactis 712 has been cloned and sequenced, le

22 to a large family of Siphoviridae and infect Lactococcus lactis, a gram-positive bacterium used in co

23 ovalently anchored in the outer cell wall of Lactococcus lactis, a Gram-positive surrogate that other

24 .4% identity to the PepF oligopeptidase from Lactococcus lactis, a member of the M3 or thimet family

25 Lactococcus lactis, a non-pathogenic bacteria, has been

26 lis and also resulted in cCF10 production by Lactococcus lactis, a non-pheromone producer.

27 Salmonella typhimurium, the ATP-PRTase from Lactococcus lactis and a number of other bacterial speci

28 ent C (TTFC) was expressed constitutively in Lactococcus lactis and administered orally to C57 BL/6 m

29 e into intact cells and membrane vesicles of Lactococcus lactis and Bacillus subtilis is strongly inh

30 d, namely that described here and those from Lactococcus lactis and Caenorhabditis elegans.

31 erfamily multidrug-proton antiporter LmrP in Lactococcus lactis and developed a novel assay for the d

32 However, the AcpAs of Lactococcus lactis and Enterococcus faecalis were inacti

33 n heterologous host systems of esp-deficient Lactococcus lactis and Enterococcus faecium did not enha

34 the interaction between probiotic bacteria (Lactococcus lactis and Escherichia coli) and A498 human

35 ts (D) in the cytoplasm of Escherichia coli, Lactococcus lactis and Haloferax volcanii.

36 pon deletion of PIC2 Additionally, assays in Lactococcus lactis and in reconstituted liposomes direct

37 Microbiological (Lactococcus lactis and Lactobacillus acidophilus counts,

38 Two natural strains of Lactococcus lactis and one mutant were characterized in

39 This TS and the TSs from Lactococcus lactis and phage Phi3T-to which it is most s

40 Certain genes from Lactococcus lactis and Pseudomonas aeruginosa, including

41 viridae that includes at least phages r1t of Lactococcus lactis and SF370.3 of Streptococcus pyogenes

42 ns and Caulobacter crescentus), and Bacilli (Lactococcus lactis and Staphylococcus aureus).

43 In Lactococcus lactis and Staphylococcus carnosus, the ilvE

44 of E. faecalis and the heterologous bacteria Lactococcus lactis and Streptococcus gordonii was demons

45 m Saccharomyces cerevisiae were expressed in Lactococcus lactis and studied in inside-out membrane ve

46 toward the bacteria Pseudomonas fluorescens, Lactococcus lactis, and 4 strains of the entomopathogen

47 Caenorhabditis elegans, Leishmania donovani, Lactococcus lactis, and Bacillus subtilis.

48 eir cross-bridge, such as Lactococcus casei, Lactococcus lactis, and Enterococcus faecium.

49 the Lactobacillus casei genome, expressed in Lactococcus lactis, and functionally characterized.

50 treptococcus mitis, Gemella parahaemolysans, Lactococcus lactis, and Fusobacterium nucleatum, were si

51 al tRNAs from the bacteria Escherichia coli, Lactococcus lactis, and Streptomyces griseus.

52 occus pyogenes, Streptococcus pneumoniae and Lactococcus lactis are analyzed for abundances of short

53 ransposition events of the Ll.LtrB intron in Lactococcus lactis are into the plasmid donor.

54 the new bacteria, Enterococcus faecalis and Lactococcus lactis, are gram positive.

55 We here report an expression system using Lactococcus lactis as a host for non-canonical amino aci

56 Ags, associated with the intake of probiotic Lactococcus lactis as tolerogenic adjuvant (combined the

57 The nisA promoter is positively regulated in Lactococcus lactis ATCC 11454 by autoinduction via a two

58 The recF gene of Lactococcus lactis ATCC 7962 is located 3 kb downstream

59 ulture of human intestinal cells with living Lactococcus lactis bacteria also was demonstrated in the

60 The collision events of single Lactococcus lactis bacteria at Pt disk ultramicroelectro

61 ned with oral gavage of genetically modified Lactococcus lactis bacteria secreting human proinsulin a

62 Low-dose anti-CD3 plus Lactococcus lactis bacteria secreting proinsulin and IL-

63 a biological membrane by expressing Gdt1p in Lactococcus lactis bacterial cells and by recording eith

64 A novel bacteriophage protection system for Lactococcus lactis based on a genetic trap, in which a s

65 athways of pyruvate metabolism of mutants of Lactococcus lactis, based on previously published experi

66 Lactococcus lactis beta-phosphoglucomutase (beta-PGM) ca

67 Activated Lactococcus lactis beta-phosphoglucomutase (betaPGM) cat

68 om YdbC, a prokaryotic PC4-like protein from Lactococcus lactis, but the underlying mechanism remains

69 e was addressed for the class 1A enzyme from Lactococcus lactis by determining kinetic isotope effect

70 superfamily multidrug transporter LmrP from Lactococcus lactis catalyses drug efflux in a membrane p

71 In Lactococcus lactis, cell-wall polysaccharides (CWPSs) ac

72 gordonii; another had 79% identity with the Lactococcus lactis clpE gene, encoding a member of the C

73 AATTTTCWGAAAATT motif, first identified for Lactococcus lactis CodY, with up to five mismatches play

74 eterologous expression of sof49 in M1 GAS or Lactococcus lactis conferred marked increases in HEp-2 c

75 Expression of the gene product in Lactococcus lactis conferred the ability to adhere to VK

76 on the surface of the non-adherent bacterium Lactococcus lactis confers adherence to scavenger recept

77 . pyogenes, when expressed on surrogate host Lactococcus lactis, confers binding to immobilized saliv

78 Here we construct synthetic Lactococcus lactis consortia and mathematical models to

79 The commercially important bacterium Lactococcus lactis contains two FNR-like proteins (FlpA

80 enetic switch of TP901-1, a bacteriophage of Lactococcus lactis, controlled by the CI repressor and t

81 three T4SS-associated, putative hydrolases, Lactococcus lactis CsiA, Tn925 Orf14, and pIP501 TraG, p

82 the drug-sensitive, Gram-positive bacterium Lactococcus lactis Delta lmrA Delta lmrCD lacking major

83 al architecture of galactose mutarotase from Lactococcus lactis determined to 1.9-A resolution.

84 -dimensional structure of galactokinase from Lactococcus lactis determined to 2.1-A resolution.

85 the survival of the non-pathogenic bacterium Lactococcus lactis during a human whole blood killing as

86 nvestigated plant habitat-specific traits of Lactococcus lactis during growth in an Arabidopsis thali

87 The conjugative element pRS01 from Lactococcus lactis encodes the putative relaxase protein

88 B. bifidum PRL2010 appendages in nonpiliated Lactococcus lactis enhanced adherence to human enterocyt

89 ble CK8 also bound to Staphylococcus aureus, Lactococcus lactis, Enterococcus faecalis, and Streptoco

90 AS in E. faecalis and the heterologous host Lactococcus lactis, experiments were designed to assess

91 mucosal-route administration of recombinant Lactococcus lactis expressing tetanus toxin fragment C (

92 gen captured on the surface of S. aureus- or Lactococcus lactis-expressing FnBPB could be activated t

93 Recent advances in the development of the Lactococcus lactis expression system have opened the way

94 A heterologous Lactococcus lactis expression system was used to express

95 4 NVDP and 38 NANP repeats) produced in the Lactococcus lactis expression system.

96 om phenotypic tests in yeast and produced in Lactococcus lactis for further biochemical characterizat

97 We examined the ability of Lactococcus lactis G121 to prevent allergic inflammatory

98 mutation to the recently solved structure of Lactococcus lactis GalK begins to provide a blueprint fo

99 l delivery in mice of biologically contained Lactococcus lactis genetically modified to secrete the w

100 nt vector (pHybrid I), a 20-kb fragment from Lactococcus lactis genomic DNA has been successfully int

101 cleoprotein (RNP) complex formed between the Lactococcus lactis group II intron and its self-encoded

102 tailed target site recognition rules for the Lactococcus lactis group II intron Ll.LtrB and to select

103 The Lactococcus lactis group II intron Ll.ltrB is similar to

104 n Escherichia coli expression system for the Lactococcus lactis group II intron Ll.LtrB to show that

105 In this work, we have trapped the native Lactococcus lactis group II intron RNP complex in its pr

106 For the pRS01 plasmid-encoded Lactococcus lactis group II intron, Ll.LtrB, splicing en

107 The genome of Lactococcus lactis has a multicistronic folate synthesis

108 ated beta-phosphoglucomutase (beta-PGM) from Lactococcus lactis has been determined to 2.3 A resoluti

109 f the PepF1 and PepF2 oligoendopeptidases of Lactococcus lactis has been identified in Bacillus subti

110 ffusion assays against the indicator strains Lactococcus lactis HP and Bacillus subtilis 6633.

111 Lactococcus lactis HR279 and JHK24 strains expressing hi

112 er of strains used in the FMP, we found that Lactococcus lactis I-1631 was sufficient to ameliorate c

113 e self-splicing group II Ll.LtrB intron from Lactococcus lactis into L. lactis 23S rRNA.

114 Previous studies of the Lactococcus lactis intron Ll.LtrB indicated that in its

115 te (ABC) transporter LmrA from the bacterium Lactococcus lactis is a homolog of the human multidrug r

116 beta-phosphoglucomutase (betaPGM) from Lactococcus lactis is a phosphoryl transfer enzyme requi

117 OpuA from Lactococcus lactis is a type I ABC-importer that uses tw

118 ss is species-specific as Acm2 purified from Lactococcus lactis is not glycosylated.

119 sus B 442, Lactobacillus rhamnosus 1937, and Lactococcus lactis JBB 500 were enriched with magnesium

120 h the nonpathogenic gram-positive bacterium, Lactococcus lactis K1, for the ability to survive in mou

121 f beta-cell autoantigens via the gut through Lactococcus lactis (L. lactis) has been demonstrated to

122 olved an efficient purification method using Lactococcus lactis (L. lactis), a generally recognized a

123 A homology model of the NADH oxidase from Lactococcus lactis (L.lac-Nox2) was also generated using

124 on Microbiology Systems) were determined for Lactococcus lactis, L. garvieae, and unknown Lactococcus

125 The Lactococcus lactis L1.LtrB intron encodes a maturase, Lt

126 er nectaris, Lactobacillus sanfranciscensis, Lactococcus lactis, Lactococcus piscium, Lactococcus pla

127 to manufacture model cheeses inoculated with Lactococcus lactis LD61.

128 lowing order: Enterococcus faecalis LDH2 </= Lactococcus lactis LDH2 < E. faecalis LDH1 < L. lactis L

129 The Lactococcus lactis Ll.LtrB group II intron encodes a rev

130 The Lactococcus lactis Ll.LtrB group II intron encodes a rev

131 Here, we analyzed the interaction of the Lactococcus lactis Ll.LtrB group II intron endonuclease

132 nalyzed DNA target-site requirements for the Lactococcus lactis Ll.LtrB group II intron in vitro and

133 The mobile Lactococcus lactis Ll.LtrB group II intron integrates in

134 The Lactococcus lactis Ll.LtrB group II intron retrohomes by

135 Here, we show that the Lactococcus lactis Ll.LtrB group II intron splices accur

136 The Lactococcus lactis Ll.LtrB group II intron uses a major

137 Here, we used databases of retargeted Lactococcus lactis Ll.LtrB group II introns and a compil

138 We previously showed that the group II Lactococcus lactis Ll.LtrB intron could retrotranspose i

139 everse transcriptase/maturase encoded by the Lactococcus lactis Ll.LtrB intron has a high affinity bi

140 site for the maturase (LtrA) encoded by the Lactococcus lactis Ll.LtrB intron is within a region of

141 Previous studies with the Lactococcus lactis Ll.LtrB intron suggested a model in w

142 Previous studies with the Lactococcus lactis Ll.LtrB intron suggested a model in w

143 e potentially involved in retrohoming of the Lactococcus lactis Ll.LtrB intron.

144 se region of the LtrA protein encoded by the Lactococcus lactis Ll.LtrB intron.

145 f homologous recombination, as found for the Lactococcus lactis Ll.LtrB intron.

146 e in C57BL/6.NOD-Aec1Aec2 (SjS) females, the Lactococcus lactis (LL) 301 strain was developed to chro

147 bacterial delivery technology based on live Lactococcus lactis (LL) bacteria for controlled secretio

148 groups of NOD mice were orally treated with Lactococcus lactis (LL) expressing CFA/I.

149 actively in situ by the food-grade bacterium Lactococcus lactis (LL-IL-27), and tested its ability to

150 The mobile group II intron of Lactococcus lactis, Ll.LtrB, provides the opportunity to

151 igate the nature of substrate binding within Lactococcus lactis LmrP, a prototypical multidrug transp

152 acilitator superfamily transporter LmrP from Lactococcus lactis mediates protonmotive-force dependent

153 The chromosome of Lactococcus lactis MG 1363 contains a 60 kb conjugative

154 ing of a human gut metagenomic library using Lactococcus lactis MG1363 as heterologous host.

155 res of two Dps proteins (DpsA and DpsB) from Lactococcus lactis MG1363 reveal for the first time the

156 Using Escherichia coli, Lactococcus lactis, Mycobacterium smegmatis, Lactobacill

157 Two candidate probiotics, Lactococcus lactis NCC 2287 and Bifidobacterium lactis N

158 n with acid-producing and non-acid producing Lactococcus lactis NCIMB 9918 in UHT milk at 30 & 18 deg

159 AbiZ causes phage phi31-infected Lactococcus lactis NCK203 to lyse 15 min early, reducing

160 n combined with pTRK391 (P15A10::lacZ.st) in Lactococcus lactis NCK203, an antisense ORF2 construct w

161 Genetically modified Lactococcus lactis, non-pathogenic bacteria expressing t

162 ctionally expressed in the heterologous host Lactococcus lactis NZ9000, and the benefits of the newly

163 eport on three such systems in the bacterium Lactococcus lactis On the basis of sequence similarities

164 Escherichia coli, Pseudomonas aeruginosa and Lactococcus lactis on the surface of the 3D models revea

165 teri, L. acidophilus, a Bifidobacterium sp., Lactococcus lactis, or a Bacillus sp. developed IBD duri

166 and functional studies on the inhibition of Lactococcus lactis PC (LlPC) by c-di-AMP.

167 purified one of these proteins, 67RuvC, from Lactococcus lactis phage bIL67 and demonstrated that it

168 es genes that are highly similar to those of Lactococcus lactis phage r1t and Streptococcus thermophi

169 also found in many bacteriophages, including Lactococcus lactis phage r1t.

170 Conjugative transfer of the Lactococcus lactis plasmid pRS01 requires splicing of a

171 nisin, simple synthetic circuits can direct Lactococcus lactis populations to form programmed spatia

172 Here we report that Lactococcus lactis possesses two different orthologues o

173 Certain strains of Lactococcus lactis produce the broad-spectrum bacterioci

174 Lactococcus lactis produces the lantibiotic nisin, which

175 otein and heterologous expression of SdrD in Lactococcus lactis promoted bacterial survival in human

176 ccharomyces cerevisiae) and in the bacterium Lactococcus lactis Protein production in these two micro

177 Heterologous expression of beta by Lactococcus lactis resulted in recruitment of FH to the

178 ging switch helix P1.1 in the representative Lactococcus lactis riboswitch.

179 catalytic module, and an endochitinase from Lactococcus lactis show that the nonprocessive enzymes h

180 colonized with recombinant PG overproducing Lactococcus lactis showed limited direct contribution of

181 vious studies in the Gram-positive bacterium Lactococcus lactis showed that heme exposure strongly in

182 Heterologous expression of Pic2 in Lactococcus lactis significantly enhanced CuL transport

183 rally-occurring plasmid pEW104 isolated from Lactococcus lactis ssp. cremoris W10.

184 The plasmid encoded LlaI R/M system from Lactococcus lactis ssp. lactis consists of a bidomain me

185 of pMRC01, a large conjugative plasmid from Lactococcus lactis ssp. lactis DPC3147, has been determi

186 small genome of the Gram-positive bacterium Lactococcus lactis ssp. lactis IL1403 contains two genes

187 ted for their antimicrobial activity against Lactococcus lactis, Staphylococcus aureus, Listeria mono

188 on, Pearson correlation analysis showed that Lactococcus lactis, Staphylococcus, Trichococcus, and Mo

189 is encoded on plasmid pJW566 and can protect Lactococcus lactis strains against bacteriophage infecti

190 Experimental evolution of several isogenic Lactococcus lactis strains demonstrated the existence of

191 Further, closely related Lactococcus lactis strains exhibited different interacti

192 Mice were then infected with Lactococcus lactis strains that differed only in SpyCEP

193 s, Listeria monocytogenes, Listeria innocua, Lactococcus lactis, Streptococcus pyogenes, Streptococcu

194 thermophiles, Lactobacillus bulgaricus, and Lactococcus lactis subsp Lactis.

195 s, including two lactic acid bacteria (i.e., Lactococcus lactis subsp.

196 Here, we report a new strain, Lactococcus lactis subsp.

197 e developed using the autochthonous cultures Lactococcus lactis subsp.

198 c amine production of two starter strains of Lactococcus lactis subsp. cremoris (strains from the Cul

199 Z32, Streptococcus thermophilus CNRZ302, and Lactococcus lactis subsp. cremoris AM2.

200 ecific integrase encoded by phage TP901-1 of Lactococcus lactis subsp. cremoris has potential as a to

201 ostoc mesenteroides subsp. jonggajibkimchii, Lactococcus lactis subsp. cremoris, Lactobacillus coryni

202 richia coli was also inhibited by 50% CFS of Lactococcus lactis subsp. lactis and 25% CFS of Leuconos

203 s were: QS - with culture Start, composed by Lactococcus lactis subsp. lactis and L. lactis subsp. cr

204 ne and 3-methyl-1-butanol were identified in Lactococcus lactis subsp. lactis and Lactococcus cremori

205 ne and 3-methyl-1-butanol were identified in Lactococcus lactis subsp. lactis and Lactococcus cremori

206 k passage structure of phage 340, a 936-type Lactococcus lactis subsp. lactis bacteriophage.

207 The native lactococcal plasmid, pKR223, from Lactococcus lactis subsp. lactis biovar diacetylactis KR

208 R2I restriction-modification (R-M) system of Lactococcus lactis subsp. lactis biovar diacetylactis KR

209 nfection immunity was conferred to the host, Lactococcus lactis subsp. lactis NCK203, indicating that

210 Recombinant HPP from Lactococcus lactis subsp. lactis that was expressed in E

211 4 residue lantibiotic produced by strains of Lactococcus lactis subsp. lactis, exerts antimicrobial a

212 aining bacteriocin (lantibiotic) produced by Lactococcus lactis subsp. lactis.

213 We assessed the effects of Lactococcus lactis subspecies (subsp) cremoris on weight

214 t constructed in the Gram-positive bacterium Lactococcus lactis subspecies lactis IL1403.

215 gative bacilli and gram-positive cocci, only Lactococcus lactis subspecies lactis produced extracellu

216 vivo performance of an engineered strain of Lactococcus lactis that altruistically degrades the wide

217 porter LmrA is a primary drug transporter in Lactococcus lactis that can functionally substitute for

218 ccine (LL-CRR) made from live, nonpathogenic Lactococcus lactis that expresses the conserved C-repeat

219 tator superfamily multidrug transporter from Lactococcus lactis that mediates the efflux of cationic

220 e is introduced into the commensal bacterium Lactococcus lactis, the truncated CBD is also produced,

221 In Lactococcus lactis there is a protein, HisZ, in the hist

222 The use of Lactococcus lactis to deliver a chosen antigen to the mu

223 erial targets, and we transfer the system to Lactococcus lactis to establish its broad functionality

224 Using a heterologous expression system in Lactococcus lactis to overcome possible staphylococcal a

225 P and FNR in Escherichia coli were sought in Lactococcus lactis to provide a basis for redirecting ca

226 oral vaccination with a probiotic organism, Lactococcus lactis, to elicit HIV-specific immune respon

227 Lactococcus lactis transformed with plasmids expressing

228 Here, we present a Lactococcus lactis Trp auxotroph-based expression system

229 In contrast, Bacillus subtilis and Lactococcus lactis use manganese, and Saccharomyces cere

230 families infect the Gram-positive bacterium Lactococcus lactis using receptor-binding proteins ancho

231 Prediction of the function of HisZ in Lactococcus lactis was assisted by comparative genomics,

232 eptococcal virulence factors from M protein, Lactococcus lactis was engineered to express M1 protein

233 Lactococcus lactis was found to be the dominant bacteriu

234 n x-ray structure of the dimeric enzyme from Lactococcus lactis was recently solved and shown to be t

235 Expression of SfbA in the noninvasive strain Lactococcus lactis was sufficient to promote fibronectin

236 e for the maintenance of this equilibrium in Lactococcus lactis, we isolated mutants that are resista

237 ptococcus mutans, Staphylococcus aureus, and Lactococcus lactis were examined for functional compleme

238 dihydroorotate dehydrogenase A (DHODA) from Lactococcus lactis, were characterized by employing sing

239 the chromosome of Lactobacillus reuteri and Lactococcus lactis without selection at frequencies rang

240 YaiB NADPH-dependent quinone reductase from Lactococcus lactis (YaiB), was developed to achieve rapi

241 Lactococcus lactis YdbC is a representative of DUF2128.

242 alculate CCRs for ~100-200 enzymes each from Lactococcus lactis, yeast, and Arabidopsis CCRs in these

243 Here, we characterize the Lactococcus lactis yybP-ykoY orphan riboswitch as a Mn(2